Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1043879
rs1043879
3 1 25243590 missense variant T/C snv 0.20 0.19 0.700 1.000 1 2011 2011
dbSNP: rs10903129
rs10903129
4 1 25442446 intron variant A/G snv 0.58 0.700 1.000 1 2011 2011
dbSNP: rs12034383
rs12034383
CR1
3 1 207630250 intron variant G/A snv 0.47 0.700 1.000 1 2011 2011
dbSNP: rs3091242
rs3091242
2 1 25348294 intron variant C/T snv 0.43 0.700 1.000 1 2011 2011
dbSNP: rs7527798
rs7527798
2 1 207698945 intron variant T/C snv 0.18 0.700 1.000 1 2011 2011